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Concepts (342)
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Concepts are derived automatically from a person's publications.
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Categories
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In this concept 'cloud', the sizes of the concepts are based not only on the number of corresponding publications, but also how relevant the concepts are to the overall topics of the publications, how long ago the publications were written, whether the person was the first or senior author, and how many other people have written about the same topic. The largest concepts are those that are most unique to this person.
4-Aminobutyrate Transaminase
Abnormalities, Multiple
Acidosis, Lactic
Adaptor Proteins, Signal Transducing
Adaptor Proteins, Vesicular Transport
Adenine Nucleotide Translocator 1
Adenosine Diphosphate
Adenosine Diphosphate Ribose
Adenosine Triphosphate
Adolescent
ADP-Ribosylation
Adult
Africa
Age of Onset
Aged
Aging, Premature
Algorithms
Alleles
Americas
Amino Acid Metabolism, Inborn Errors
Amino Acid Sequence
Amino Acid Substitution
Animals
Antiporters
Arabs
Arrhythmias, Cardiac
Arylamine N-Acetyltransferase
Asia
Ataxia Telangiectasia
Ataxia Telangiectasia Mutated Proteins
ATP-Dependent Proteases
Base Sequence
Biomarkers
Biopsy
Bone and Bones
Brain
Brain Diseases
Brain Stem
Breast Neoplasms
Calcium Channels
Calcium-Binding Proteins
Canada
Cardiomyopathies
Cardiomyopathy, Hypertrophic
Cardiovascular Diseases
Carnitine
Case-Control Studies
Cataract
Cell Cycle Proteins
Cell Death
Cell Line
Cell Line, Transformed
Cell Line, Tumor
Cells, Cultured
Cerebellar Ataxia
Chenodeoxycholic Acid
Child
Child, Preschool
Cholestanetriol 26-Monooxygenase
Cholestanol
Cholestasis
Cholesterol
Cholesterol, HDL
Chromatography, Liquid
Chromosome Mapping
Chromosome Segregation
Chromosomes, Human, Pair 2
Chromosomes, Human, Y
Chronic Disease
Cilia
Citric Acid Cycle
Class I Phosphatidylinositol 3-Kinases
Codon
Cohort Studies
Computational Biology
Connective Tissue Diseases
Consanguinity
Craniofacial Abnormalities
Craniosynostoses
Cutis Laxa
Cytochrome-c Oxidase Deficiency
Cytoskeletal Proteins
Databases, Genetic
Developmental Disabilities
Diabetes Mellitus
Diagnosis, Differential
Diarrhea
Disease Progression
DNA Copy Number Variations
DNA Helicases
DNA Mutational Analysis
DNA Replication
DNA, Mitochondrial
DNA-Binding Proteins
DNA-Directed RNA Polymerases
Down-Regulation
Drosophila
Ductus Arteriosus, Patent
Dyskeratosis Congenita
Dyslipidemias
Ectodermal Dysplasia
Electron Transport
Electron Transport Chain Complex Proteins
Electron Transport Complex I
Electron Transport Complex IV
Endoplasmic Reticulum Stress
Energy Metabolism
Enoyl-CoA Hydratase
Enzyme Activation
Epilepsy
Eukaryotic Initiation Factor-2
Europe
Evolution, Molecular
Exome
Exons
Exoribonucleases
Facial Asymmetry
Family
Fatal Outcome
F-Box Proteins
Female
Fetal Growth Retardation
Fibroblasts
Flumazenil
Follow-Up Studies
Fumarates
GABA Modulators
gamma-Aminobutyric Acid
gamma-Glutamyltransferase
Gene Deletion
Gene Dosage
Gene Expression
Gene Expression Regulation
Gene Frequency
Gene Pool
Genes, Dominant
Genes, Mitochondrial
Genes, Neoplasm
Genes, Recessive
Genetic Association Studies
Genetic Complementation Test
Genetic Diseases, X-Linked
Genetic Loci
Genetic Markers
Genetic Predisposition to Disease
Genetic Variation
Genetics, Medical
Genetics, Population
Genome, Human
Genome, Viral
Genomic Structural Variation
Genotype
Geography
Glycoside Hydrolases
Golgi Apparatus
Growth Disorders
Haplotypes
Heart Defects, Congenital
Hedgehog Proteins
HEK293 Cells
Heme
Heterografts
High-Temperature Requirement A Serine Peptidase 2
High-Throughput Nucleotide Sequencing
HLA Antigens
Hominidae
Homozygote
Human Genome Project
Humans
Hydrogen Peroxide
Hydroxymethyl and Formyl Transferases
Hyperglycemia
Hypertension
Hypertrichosis
Immunoblotting
Immunologic Deficiency Syndromes
Incidence
Infant
Infant, Newborn
Inheritance Patterns
Intellectual Disability
Intracellular Signaling Peptides and Proteins
Introns
Iron-Sulfur Proteins
Isoenzymes
Kinetics
Language Development Disorders
Learning
Leigh Disease
Leukoencephalopathies
Linkage Disequilibrium
Liver Failure, Acute
Longitudinal Studies
Long-Term Synaptic Depression
Loss of Function Mutation
Lymphoma
Lysogeny
Magnetic Resonance Imaging
Malate Dehydrogenase
Malates
Male
Mass Spectrometry
Mechanistic Target of Rapamycin Complex 1
Membrane Potential, Mitochondrial
Memory
Metabolic Networks and Pathways
Metabolism, Inborn Errors
Metabolome
Metabolomics
Mice
Mice, Inbred C57BL
Mice, Knockout
Mice, Nude
Mice, Transgenic
Microbiota
Microcephaly
Micronesia
MicroRNAs
Middle Aged
Mitochondria
Mitochondrial Diseases
Mitochondrial Encephalomyopathies
Mitochondrial Proteins
Mitochondrial Proton-Translocating ATPases
Models, Molecular
Molecular Chaperones
Molecular Sequence Data
Morphogenesis
Multifunctional Enzymes
Muscle Hypotonia
Muscle Weakness
Muscle, Skeletal
Mutagenesis, Insertional
Mutagenesis, Site-Directed
Mutation
Mutation, Missense
NADH Dehydrogenase
Neonatal Screening
Neoplasm Proteins
Neoplasms
Nephrolithiasis
Nerve Degeneration
Nerve Tissue Proteins
Nervous System Diseases
Nervous System Malformations
Neurodegenerative Diseases
Neurodevelopmental Disorders
Neuroimaging
Nonsense Mediated mRNA Decay
Nuclear Proteins
Nucleosides
Nucleotides
Obesity
Oculocerebrorenal Syndrome
Oxidative Phosphorylation
Oxidative Stress
Pantothenate Kinase-Associated Neurodegeneration
Pedigree
Penetrance
Peptide Elongation Factor Tu
Peptide Elongation Factors
Peptides
Phenotype
Phosphatidylinositol 3-Kinase
Phosphatidylinositol 3-Kinases
Phosphoric Monoester Hydrolases
Phosphorylation
Phosphotransferases (Alcohol Group Acceptor)
Phylogeny
Polymerase Chain Reaction
Polymorphism, Single Nucleotide
Population Groups
Population Surveillance
Precision Medicine
Prevalence
Progeria
Prognosis
Protein Binding
Protein Biosynthesis
Protein Conformation
Protein Domains
Protein Interaction Domains and Motifs
Protein Processing, Post-Translational
Protein Subunits
Protein Transport
Proteins
Proteolysis
Pseudogenes
Rabbits
Receptors, AMPA
Receptors, Metabotropic Glutamate
Recombination, Genetic
Retrospective Studies
Rhabdomyolysis
Ribonucleoside Diphosphate Reductase
Ribonucleotide Reductases
RNA Helicases
RNA Processing, Post-Transcriptional
RNA, Messenger
RNA, Ribosomal, 16S
RNA, Transfer
RNA-Binding Proteins
Seizures
Sequence Analysis, DNA
Sequence Deletion
Sequence Homology
Sequence Homology, Amino Acid
Serine Proteases
Sex Factors
Siblings
Software
Space Perception
Spastic Paraplegia, Hereditary
Spinocerebellar Ataxias
Spinocerebellar Degenerations
Staphylococcus epidermidis
Staphylococcus Phages
Structure-Activity Relationship
Substrate Specificity
Survival Rate
Syndrome
Tandem Mass Spectrometry
Telomere Shortening
Tetraspanins
Thiolester Hydrolases
Time Factors
Transcription Factors
Transcription, Genetic
Transduction, Genetic
Triglycerides
Trinucleotide Repeats
Tumor Suppressor Proteins
Ubiquinone
Ubiquitin-Protein Ligases
Valine
Valine-tRNA Ligase
Virus Assembly
X Chromosome
Xanthomatosis
Xanthomatosis, Cerebrotendinous
Young Adult
Zebrafish
BONNEN's Networks
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Concepts (342)
Derived automatically from this person's publications.
Mutation
Mitochondrial Proteins
DNA, Mitochondrial
Mitochondrial Encephalomyopathies
Mitochondrial Diseases
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Co-Authors (42)
People in Profiles who have published with this person.
BACINO, CARLOS
CRAIGEN, WILLIAM
NELSON, DAVID
LALANI, SEEMA
COSTA-MATTIOLI, MAURO
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Similar People (60)
People who share similar concepts with this person.
LUPSKI, JAMES
BOERWINKLE, ERIC
GIBBS, RICHARD
AMOS, CHRIS
SCAGLIA, FERNANDO
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_
Same Department
People who are also in this person's primary department.
CRAIGEN, WILLIAM
GKOUNTAROULIS, DIMOS
KLISCH, TIEMO
LIU, NING
MUZNY, DONNA
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Physical Neighbors
People whose addresses are nearby this person.
ELLIS, LAURA
ELSEA, SARAH
HAELTERMAN, NELE
HARRIS, RONALD
PARK, DONGSU
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